CA2970801A1 - Acides nucleiques double brin modifies par un ligand - Google Patents
Acides nucleiques double brin modifies par un ligand Download PDFInfo
- Publication number
- CA2970801A1 CA2970801A1 CA2970801A CA2970801A CA2970801A1 CA 2970801 A1 CA2970801 A1 CA 2970801A1 CA 2970801 A CA2970801 A CA 2970801A CA 2970801 A CA2970801 A CA 2970801A CA 2970801 A1 CA2970801 A1 CA 2970801A1
- Authority
- CA
- Canada
- Prior art keywords
- dsna
- nucleotides
- nucleotide
- strand
- ligand
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 150000007523 nucleic acids Chemical class 0.000 title claims abstract description 140
- 102000039446 nucleic acids Human genes 0.000 title claims abstract description 125
- 108020004707 nucleic acids Proteins 0.000 title claims abstract description 125
- 125000003729 nucleotide group Chemical group 0.000 claims abstract description 823
- 239000002773 nucleotide Substances 0.000 claims abstract description 676
- 230000000692 anti-sense effect Effects 0.000 claims abstract description 503
- 239000003446 ligand Substances 0.000 claims abstract description 220
- 238000000034 method Methods 0.000 claims abstract description 34
- 108091028664 Ribonucleotide Proteins 0.000 claims description 346
- 239000002336 ribonucleotide Substances 0.000 claims description 346
- 108091081021 Sense strand Proteins 0.000 claims description 341
- 125000002652 ribonucleotide group Chemical group 0.000 claims description 259
- 125000002637 deoxyribonucleotide group Chemical group 0.000 claims description 194
- 239000005547 deoxyribonucleotide Substances 0.000 claims description 190
- 238000012986 modification Methods 0.000 claims description 132
- 230000004048 modification Effects 0.000 claims description 130
- 238000003776 cleavage reaction Methods 0.000 claims description 126
- 230000007017 scission Effects 0.000 claims description 125
- -1 dimethoxytrityl Chemical group 0.000 claims description 99
- 108091032973 (ribonucleotides)n+m Chemical class 0.000 claims description 89
- 230000000295 complement effect Effects 0.000 claims description 70
- MBLBDJOUHNCFQT-UHFFFAOYSA-N N-acetyl-D-galactosamine Natural products CC(=O)NC(C=O)C(O)C(O)C(O)CO MBLBDJOUHNCFQT-UHFFFAOYSA-N 0.000 claims description 52
- 239000000758 substrate Substances 0.000 claims description 51
- 210000004027 cell Anatomy 0.000 claims description 48
- RYYWUUFWQRZTIU-UHFFFAOYSA-K thiophosphate Chemical compound [O-]P([O-])([O-])=S RYYWUUFWQRZTIU-UHFFFAOYSA-K 0.000 claims description 48
- 235000000346 sugar Nutrition 0.000 claims description 39
- HVYWMOMLDIMFJA-DPAQBDIFSA-N cholesterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2 HVYWMOMLDIMFJA-DPAQBDIFSA-N 0.000 claims description 38
- 230000014509 gene expression Effects 0.000 claims description 38
- 108090000623 proteins and genes Proteins 0.000 claims description 33
- 230000027455 binding Effects 0.000 claims description 32
- OVRNDRQMDRJTHS-CBQIKETKSA-N N-Acetyl-D-Galactosamine Chemical compound CC(=O)N[C@H]1[C@@H](O)O[C@H](CO)[C@H](O)[C@@H]1O OVRNDRQMDRJTHS-CBQIKETKSA-N 0.000 claims description 30
- 208000035657 Abasia Diseases 0.000 claims description 26
- 230000001965 increasing effect Effects 0.000 claims description 25
- OVRNDRQMDRJTHS-KEWYIRBNSA-N N-acetyl-D-galactosamine Chemical compound CC(=O)N[C@H]1C(O)O[C@H](CO)[C@H](O)[C@@H]1O OVRNDRQMDRJTHS-KEWYIRBNSA-N 0.000 claims description 24
- 101710163270 Nuclease Proteins 0.000 claims description 20
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- 102000005427 Asialoglycoprotein Receptor Human genes 0.000 claims description 16
- 108010006523 asialoglycoprotein receptor Proteins 0.000 claims description 16
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- 235000019152 folic acid Nutrition 0.000 claims description 13
- 239000011724 folic acid Substances 0.000 claims description 13
- FDGQSTZJBFJUBT-UHFFFAOYSA-N hypoxanthine Chemical compound O=C1NC=NC2=C1NC=N2 FDGQSTZJBFJUBT-UHFFFAOYSA-N 0.000 claims description 12
- 150000003013 phosphoric acid derivatives Chemical class 0.000 claims description 11
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- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 10
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- 102000004169 proteins and genes Human genes 0.000 claims description 10
- ZSKGQVFRTSEPJT-UHFFFAOYSA-N pyrrole-2-carboxaldehyde Chemical compound O=CC1=CC=CN1 ZSKGQVFRTSEPJT-UHFFFAOYSA-N 0.000 claims description 10
- 241000894007 species Species 0.000 claims description 10
- 230000008685 targeting Effects 0.000 claims description 10
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 9
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- HMFHBZSHGGEWLO-UHFFFAOYSA-N alpha-D-Furanose-Ribose Natural products OCC1OC(O)C(O)C1O HMFHBZSHGGEWLO-UHFFFAOYSA-N 0.000 claims description 9
- 230000001976 improved effect Effects 0.000 claims description 8
- YACKEPLHDIMKIO-UHFFFAOYSA-N methylphosphonic acid Chemical compound CP(O)(O)=O YACKEPLHDIMKIO-UHFFFAOYSA-N 0.000 claims description 8
- 108090000765 processed proteins & peptides Proteins 0.000 claims description 8
- PYMYPHUHKUWMLA-UHFFFAOYSA-N arabinose Natural products OCC(O)C(O)C(O)C=O PYMYPHUHKUWMLA-UHFFFAOYSA-N 0.000 claims description 7
- SRBFZHDQGSBBOR-UHFFFAOYSA-N beta-D-Pyranose-Lyxose Natural products OC1COC(O)C(O)C1O SRBFZHDQGSBBOR-UHFFFAOYSA-N 0.000 claims description 7
- YBJHBAHKTGYVGT-ZKWXMUAHSA-N (+)-Biotin Chemical compound N1C(=O)N[C@@H]2[C@H](CCCCC(=O)O)SC[C@@H]21 YBJHBAHKTGYVGT-ZKWXMUAHSA-N 0.000 claims description 6
- GVJHHUAWPYXKBD-UHFFFAOYSA-N (±)-α-Tocopherol Chemical compound OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-UHFFFAOYSA-N 0.000 claims description 6
- LQLQRFGHAALLLE-UHFFFAOYSA-N 5-bromouracil Chemical compound BrC1=CNC(=O)NC1=O LQLQRFGHAALLLE-UHFFFAOYSA-N 0.000 claims description 6
- HMFHBZSHGGEWLO-SOOFDHNKSA-N D-ribofuranose Chemical compound OC[C@H]1OC(O)[C@H](O)[C@@H]1O HMFHBZSHGGEWLO-SOOFDHNKSA-N 0.000 claims description 6
- SRBFZHDQGSBBOR-IOVATXLUSA-N D-xylopyranose Chemical compound O[C@@H]1COC(O)[C@H](O)[C@H]1O SRBFZHDQGSBBOR-IOVATXLUSA-N 0.000 claims description 6
- 108020004414 DNA Proteins 0.000 claims description 6
- UGQMRVRMYYASKQ-UHFFFAOYSA-N Hypoxanthine nucleoside Natural products OC1C(O)C(CO)OC1N1C(NC=NC2=O)=C2N=C1 UGQMRVRMYYASKQ-UHFFFAOYSA-N 0.000 claims description 6
- SMEROWZSTRWXGI-UHFFFAOYSA-N Lithocholsaeure Natural products C1CC2CC(O)CCC2(C)C2C1C1CCC(C(CCC(O)=O)C)C1(C)CC2 SMEROWZSTRWXGI-UHFFFAOYSA-N 0.000 claims description 6
- RADKZDMFGJYCBB-UHFFFAOYSA-N Pyridoxal Chemical compound CC1=NC=C(CO)C(C=O)=C1O RADKZDMFGJYCBB-UHFFFAOYSA-N 0.000 claims description 6
- 230000004700 cellular uptake Effects 0.000 claims description 6
- 238000009826 distribution Methods 0.000 claims description 6
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 claims description 6
- SMEROWZSTRWXGI-HVATVPOCSA-N lithocholic acid Chemical compound C([C@H]1CC2)[C@H](O)CC[C@]1(C)[C@@H]1[C@@H]2[C@@H]2CC[C@H]([C@@H](CCC(O)=O)C)[C@@]2(C)CC1 SMEROWZSTRWXGI-HVATVPOCSA-N 0.000 claims description 6
- 150000002894 organic compounds Chemical class 0.000 claims description 6
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 6
- XUARCIYIVXVTAE-ZAPOICBTSA-N uvaol Chemical compound C1C[C@H](O)C(C)(C)[C@@H]2CC[C@@]3(C)[C@]4(C)CC[C@@]5(CO)CC[C@@H](C)[C@H](C)[C@H]5C4=CC[C@@H]3[C@]21C XUARCIYIVXVTAE-ZAPOICBTSA-N 0.000 claims description 6
- XQCZBXHVTFVIFE-UHFFFAOYSA-N 2-amino-4-hydroxypyrimidine Chemical compound NC1=NC=CC(O)=N1 XQCZBXHVTFVIFE-UHFFFAOYSA-N 0.000 claims description 5
- MWBWWFOAEOYUST-UHFFFAOYSA-N 2-aminopurine Chemical compound NC1=NC=C2N=CNC2=N1 MWBWWFOAEOYUST-UHFFFAOYSA-N 0.000 claims description 5
- PHAFOFIVSNSAPQ-UHFFFAOYSA-N 4-fluoro-6-methyl-1h-benzimidazole Chemical compound CC1=CC(F)=C2NC=NC2=C1 PHAFOFIVSNSAPQ-UHFFFAOYSA-N 0.000 claims description 5
- QCXGJTGMGJOYDP-UHFFFAOYSA-N 4-methyl-1h-benzimidazole Chemical compound CC1=CC=CC2=C1N=CN2 QCXGJTGMGJOYDP-UHFFFAOYSA-N 0.000 claims description 5
- QCHLWIPINNRBSG-UHFFFAOYSA-N 6-thiophen-2-yl-7h-purin-2-amine Chemical compound C=12NC=NC2=NC(N)=NC=1C1=CC=CS1 QCHLWIPINNRBSG-UHFFFAOYSA-N 0.000 claims description 5
- ORILYTVJVMAKLC-UHFFFAOYSA-N adamantane Chemical compound C1C(C2)CC3CC1CC2C3 ORILYTVJVMAKLC-UHFFFAOYSA-N 0.000 claims description 5
- 125000002178 anthracenyl group Chemical group C1(=CC=CC2=CC3=CC=CC=C3C=C12)* 0.000 claims description 5
- 230000021615 conjugation Effects 0.000 claims description 5
- 210000004962 mammalian cell Anatomy 0.000 claims description 5
- 238000004519 manufacturing process Methods 0.000 claims description 5
- 230000003278 mimic effect Effects 0.000 claims description 5
- 239000002777 nucleoside Substances 0.000 claims description 5
- 150000003833 nucleoside derivatives Chemical class 0.000 claims description 5
- 125000003933 pentacenyl group Chemical group C1(=CC=CC2=CC3=CC4=CC5=CC=CC=C5C=C4C=C3C=C12)* 0.000 claims description 5
- 125000001725 pyrenyl group Chemical group 0.000 claims description 5
- 230000002194 synthesizing effect Effects 0.000 claims description 5
- 125000001935 tetracenyl group Chemical group C1(=CC=CC2=CC3=CC4=CC=CC=C4C=C3C=C12)* 0.000 claims description 5
- 229940075420 xanthine Drugs 0.000 claims description 5
- 230000003247 decreasing effect Effects 0.000 claims description 4
- 125000004573 morpholin-4-yl group Chemical group N1(CCOCC1)* 0.000 claims description 4
- NOOLISFMXDJSKH-UTLUCORTSA-N (+)-Neomenthol Chemical group CC(C)[C@@H]1CC[C@@H](C)C[C@@H]1O NOOLISFMXDJSKH-UTLUCORTSA-N 0.000 claims description 3
- DTGKSKDOIYIVQL-WEDXCCLWSA-N (+)-borneol Chemical group C1C[C@@]2(C)[C@@H](O)C[C@@H]1C2(C)C DTGKSKDOIYIVQL-WEDXCCLWSA-N 0.000 claims description 3
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- REPVLJRCJUVQFA-UHFFFAOYSA-N (-)-isopinocampheol Chemical group C1C(O)C(C)C2C(C)(C)C1C2 REPVLJRCJUVQFA-UHFFFAOYSA-N 0.000 claims description 3
- HSINOMROUCMIEA-FGVHQWLLSA-N (2s,4r)-4-[(3r,5s,6r,7r,8s,9s,10s,13r,14s,17r)-6-ethyl-3,7-dihydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1h-cyclopenta[a]phenanthren-17-yl]-2-methylpentanoic acid Chemical compound C([C@@]12C)C[C@@H](O)C[C@H]1[C@@H](CC)[C@@H](O)[C@@H]1[C@@H]2CC[C@]2(C)[C@@H]([C@H](C)C[C@H](C)C(O)=O)CC[C@H]21 HSINOMROUCMIEA-FGVHQWLLSA-N 0.000 claims description 3
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- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
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- 238000011068 loading method Methods 0.000 description 1
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- 210000001161 mammalian embryo Anatomy 0.000 description 1
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- 239000002207 metabolite Substances 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 238000000386 microscopy Methods 0.000 description 1
- 235000019799 monosodium phosphate Nutrition 0.000 description 1
- 230000008450 motivation Effects 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- 239000013642 negative control Substances 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 108091027963 non-coding RNA Proteins 0.000 description 1
- 102000042567 non-coding RNA Human genes 0.000 description 1
- 125000005187 nonenyl group Chemical group C(=CCCCCCCC)* 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 125000001400 nonyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000005071 nonynyl group Chemical group C(#CCCCCCCC)* 0.000 description 1
- 229940127073 nucleoside analogue Drugs 0.000 description 1
- 125000004365 octenyl group Chemical group C(=CCCCCCC)* 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000005069 octynyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C#C* 0.000 description 1
- 108010092948 oligonucleotidase Proteins 0.000 description 1
- 125000002255 pentenyl group Chemical group C(=CCCC)* 0.000 description 1
- 125000004115 pentoxy group Chemical group [*]OC([H])([H])C([H])([H])C([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
- 125000005981 pentynyl group Chemical group 0.000 description 1
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- 239000002953 phosphate buffered saline Substances 0.000 description 1
- 150000008298 phosphoramidates Chemical class 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 239000013641 positive control Substances 0.000 description 1
- 238000012805 post-processing Methods 0.000 description 1
- 230000001124 posttranscriptional effect Effects 0.000 description 1
- 239000004224 potassium gluconate Substances 0.000 description 1
- 235000013926 potassium gluconate Nutrition 0.000 description 1
- 229960003189 potassium gluconate Drugs 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 239000013615 primer Substances 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 125000004368 propenyl group Chemical group C(=CC)* 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- MWWATHDPGQKSAR-UHFFFAOYSA-N propyne Chemical compound CC#C MWWATHDPGQKSAR-UHFFFAOYSA-N 0.000 description 1
- 125000002568 propynyl group Chemical group [*]C#CC([H])([H])[H] 0.000 description 1
- PTJWIQPHWPFNBW-GBNDHIKLSA-N pseudouridine Chemical compound O[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1C1=CNC(=O)NC1=O PTJWIQPHWPFNBW-GBNDHIKLSA-N 0.000 description 1
- IGFXRKMLLMBKSA-UHFFFAOYSA-N purine Chemical compound N1=C[N]C2=NC=NC2=C1 IGFXRKMLLMBKSA-UHFFFAOYSA-N 0.000 description 1
- 125000000561 purinyl group Chemical group N1=C(N=C2N=CNC2=C1)* 0.000 description 1
- 230000002285 radioactive effect Effects 0.000 description 1
- 102000016914 ras Proteins Human genes 0.000 description 1
- 108010014186 ras Proteins Proteins 0.000 description 1
- 230000010837 receptor-mediated endocytosis Effects 0.000 description 1
- 230000003252 repetitive effect Effects 0.000 description 1
- 108020004418 ribosomal RNA Proteins 0.000 description 1
- DWRXFEITVBNRMK-JXOAFFINSA-N ribothymidine Chemical compound O=C1NC(=O)C(C)=CN1[C@H]1[C@H](O)[C@H](O)[C@@H](CO)O1 DWRXFEITVBNRMK-JXOAFFINSA-N 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000012216 screening Methods 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 230000011664 signaling Effects 0.000 description 1
- AJPJDKMHJJGVTQ-UHFFFAOYSA-M sodium dihydrogen phosphate Chemical compound [Na+].OP(O)([O-])=O AJPJDKMHJJGVTQ-UHFFFAOYSA-M 0.000 description 1
- 229910000162 sodium phosphate Inorganic materials 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 230000000392 somatic effect Effects 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 210000000130 stem cell Anatomy 0.000 description 1
- 125000005346 substituted cycloalkyl group Chemical group 0.000 description 1
- 150000008163 sugars Chemical class 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 208000024891 symptom Diseases 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- ABZLKHKQJHEPAX-UHFFFAOYSA-N tetramethylrhodamine Chemical compound C=12C=CC(N(C)C)=CC2=[O+]C2=CC(N(C)C)=CC=C2C=1C1=CC=CC=C1C([O-])=O ABZLKHKQJHEPAX-UHFFFAOYSA-N 0.000 description 1
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- 125000004784 trichloromethoxy group Chemical group ClC(O*)(Cl)Cl 0.000 description 1
- 239000013638 trimer Substances 0.000 description 1
- 238000009281 ultraviolet germicidal irradiation Methods 0.000 description 1
- DJJCXFVJDGTHFX-XVFCMESISA-N uridine 5'-monophosphate Chemical compound O[C@@H]1[C@H](O)[C@@H](COP(O)(O)=O)O[C@H]1N1C(=O)NC(=O)C=C1 DJJCXFVJDGTHFX-XVFCMESISA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
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- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H21/00—Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids
- C07H21/04—Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids with deoxyribosyl as saccharide radical
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- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/50—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
- A61K47/51—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
- A61K47/54—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an organic compound
- A61K47/549—Sugars, nucleosides, nucleotides or nucleic acids
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
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- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
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- C12N15/09—Recombinant DNA-technology
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- C12N15/09—Recombinant DNA-technology
- C12N15/11—DNA or RNA fragments; Modified forms thereof; Non-coding nucleic acids having a biological activity
- C12N15/113—Non-coding nucleic acids modulating the expression of genes, e.g. antisense oligonucleotides; Antisense DNA or RNA; Triplex- forming oligonucleotides; Catalytic nucleic acids, e.g. ribozymes; Nucleic acids used in co-suppression or gene silencing
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- C12N2310/35—Nature of the modification
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- C12N2310/3515—Lipophilic moiety, e.g. cholesterol
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Abstract
L'invention porte sur des molécules d'acide nucléique double brin comprenant une extension 5' du brin sens ou antisens et comprenant en outre une pluralité de nucléotides qui sont conjugués à un ligand et sur des procédés d'utilisation des molécules d'acide nucléique double brin. Des oligomères modifiés par un ligand dans lesquels les brins sens forment une tétraboucle permettent d'obtenir de nouveaux agents d'interférence ARN puissants et stables. Ces molécules d'ANdb sont synthétisées à l'aide d'une pluralité de nucléotides qui comprennent des monomères modifiés par un ligand, des monomères analogues nucléotidiques, des monomères nucléotidiques modifiés et similaires, à l'aide de procédés et systèmes de synthèse de nucléotides standard.
Applications Claiming Priority (9)
Application Number | Priority Date | Filing Date | Title |
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US201462092241P | 2014-12-15 | 2014-12-15 | |
US201462092238P | 2014-12-15 | 2014-12-15 | |
US62/092,238 | 2014-12-15 | ||
US62/092,241 | 2014-12-15 | ||
US201562187856P | 2015-07-02 | 2015-07-02 | |
US201562187848P | 2015-07-02 | 2015-07-02 | |
US62/187,848 | 2015-07-02 | ||
US62/187,856 | 2015-07-02 | ||
PCT/US2015/065906 WO2016100401A1 (fr) | 2014-12-15 | 2015-12-15 | Acides nucléiques double brin modifiés par un ligand |
Publications (2)
Publication Number | Publication Date |
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CA2970801A1 true CA2970801A1 (fr) | 2016-06-23 |
CA2970801C CA2970801C (fr) | 2024-02-13 |
Family
ID=56127491
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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CA2970801A Active CA2970801C (fr) | 2014-12-15 | 2015-12-15 | Acides nucleiques double brin modifies par un ligand |
Country Status (8)
Country | Link |
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US (2) | US20170305956A1 (fr) |
EP (3) | EP3865576A1 (fr) |
JP (1) | JP7105065B2 (fr) |
AU (2) | AU2015362630B2 (fr) |
CA (1) | CA2970801C (fr) |
DK (2) | DK3234132T3 (fr) |
ES (2) | ES2747842T3 (fr) |
WO (1) | WO2016100401A1 (fr) |
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JP6688292B2 (ja) | 2014-10-10 | 2020-04-28 | ダイセルナ ファーマシューティカルズ, インコーポレイテッドDicerna Pharmaceuticals, Inc. | 乳酸デヒドロゲナーゼ及びその薬剤の治療的阻害 |
CN110072530A (zh) | 2016-09-02 | 2019-07-30 | 迪克纳制药公司 | 4′-磷酸酯类似物和包含其的寡核苷酸 |
BR112019008856A2 (pt) * | 2016-11-07 | 2019-07-09 | nanoSUR LLC | rnas de fita dupla quimicamente modificados pós-transcricionalmente |
AU2017368050A1 (en) | 2016-11-29 | 2019-06-20 | Puretech Lyt, Inc. | Exosomes for delivery of therapeutic agents |
WO2019006375A1 (fr) * | 2017-06-29 | 2019-01-03 | Dicerna Pharmaceuticals, Inc. | Compositions et procédés pour inhiber l'expression de hmgb1 |
KR102609396B1 (ko) * | 2017-10-13 | 2023-12-01 | 노보 노르디스크 헬스 케어 악티엔게젤샤프트 | Ldha의 발현을 억제하기 위한 방법 및 조성물 |
CN111225922B (zh) * | 2017-10-18 | 2023-07-18 | 迪克纳制药公司 | β连环蛋白核酸抑制剂分子 |
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CA3086409A1 (fr) * | 2018-01-16 | 2019-07-25 | Dicerna Pharmaceuticals, Inc. | Compositions et methodes pour inhiber l'expression de l'aldh2 |
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KR20200144100A (ko) | 2018-04-13 | 2020-12-28 | 다이서나 파마수이티컬, 인크. | Tm-증가 뉴클레오타이드로 변형된 이중-가닥 핵산 억제제 분자 |
JP7384833B2 (ja) * | 2018-05-16 | 2023-11-21 | アルニラム・ファーマシューティカルズ・インコーポレーテッド | オフターゲット効果が低下した修飾rna剤 |
EP3844279A4 (fr) * | 2018-08-27 | 2022-06-01 | Sirnaomics, Inc. | Produits et compositions |
CN112805294A (zh) | 2018-09-28 | 2021-05-14 | 胡桃钳医疗公司 | 用于核酸递送的叔氨基脂化的阳离子肽 |
MX2021007001A (es) * | 2018-12-12 | 2021-10-13 | Dicerna Pharmaceuticals Inc | Moleculas inhibidoras de acido nucleico de cadena doble que contienen un tribucle. |
SG11202106857VA (en) * | 2018-12-28 | 2021-07-29 | Dicerna Pharmaceuticals Inc | Compositions and methods for inhibiting hmgb1 expression |
JP2023501020A (ja) * | 2018-12-28 | 2023-01-18 | サーナオミクス インコーポレイテッド | 治療用分子の標的化送達 |
MX2021009754A (es) | 2019-02-12 | 2021-09-08 | Dicerna Pharmaceuticals Inc | Metodos y composiciones para inhibir la expresion de cyp27a1. |
CN113924365A (zh) | 2019-03-29 | 2022-01-11 | 迪克纳制药公司 | 用于治疗kras相关疾病或病症的组合物和方法 |
US20220170025A1 (en) | 2019-04-04 | 2022-06-02 | Dicerna Pharmaceuticals Inc. | Compositions and methods for inhibiting gene expression in the central nervous system |
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EP3234132A1 (fr) | 2017-10-25 |
EP3234132B1 (fr) | 2019-07-10 |
ES2747842T3 (es) | 2020-03-11 |
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